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Research 931–960 of 1000+
- Dermatological concerns for women and girls with turner syndrome
- Bicalutamide: A review
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- A phase 2a study investigating the effects of ritlecitinib on brainstem auditory evoked potentials and intraepidermal nerve fiber histology in adults with alopecia areata
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Homozygous whole body <i>Cbs</i> knockout in adult mice features minimal pathology during ageing despite severe homocysteinemia
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- FOXP3 <sup>+</sup> regulatory T cells and age‐related diseases
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- The Effects of Androgens on T Cells: Clues to Female Predominance in Autoimmune Liver Diseases?
- Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss
- Sperm extraction in nonmosaic Klinefelter syndrome patients: A case series and literature review of sperm extraction in Klinefelter syndrome patients
- Efficacy of metformin therapy in adolescent girls with androgen excess: relation to sex hormone–binding globulin and androgen receptor polymorphisms
- The role of 5-α-reductase inhibition in supressing progression of male androgenetic alopecia − a postulate for further studies on possible application of saw palmetto extracts
- How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns
- Resident Memory T Cells in Autoimmune Skin Diseases
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate
- Stereotactic Body Radiation Therapy As a Derivative of Stereotactic Radiosurgery: Clinically Independent But With Enduring Common Themes
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- The First Visit: Consult and Workup Before Sperm Banking
- A Novel Marker of Tissue Junctions, Collagen XXII
- Human hair keratin-associated proteins: Sequence regularities and structural implications